|Publication number||US7253004 B2|
|Application number||US 10/197,905|
|Publication date||Aug 7, 2007|
|Filing date||Jul 18, 2002|
|Priority date||Jul 19, 2001|
|Also published as||CA2393739A1, CA2393739C, CN1402000A, DE60144014D1, EP1278061A1, EP1278061B1, US20030109056|
|Publication number||10197905, 197905, US 7253004 B2, US 7253004B2, US-B2-7253004, US7253004 B2, US7253004B2|
|Inventors||Tobias Vossmeyer, Akio Yasuda, Roland E. Bauer, Klaus Müllen|
|Original Assignee||Sony Deutschland Gmbh|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (10), Non-Patent Citations (29), Referenced by (23), Classifications (23), Legal Events (8)|
|External Links: USPTO, USPTO Assignment, Espacenet|
The invention relates to a chemical sensor, a method for obtaining such chemical sensor and a method for detecting an analyte by using said chemical sensor.
In recent years much effort has been made to develop devices, which mimic the sense of smell or taste. Such devices, which are usually called electronic noses and electronic tongues, respectively, would be well suited for a broad variety of applications, such as entertainment robots, identification systems, quality control systems, environmental monitoring, and medical diagnostics. However, up to now only a limited number of electronic nose devices have been marketed. Although these devices are capable of identifying or classifying some “odor” samples, further improvements are necessary to fulfil the needs for many advanced applications mentioned above. These applications often require higher sensitivity, higher discrimination capability, faster response, better stability, and lower power consumption. Since such features strongly depend on the characteristics of the chemical sensors used in the device, there is a strong demand for improved sensors meeting the requirements for advanced e-nose and e-tongue applications.
During the past few years new kinds of chemical sensors have been developed based on organic/inorganic composite materials. In general these materials consist of an organic matrix comprising inorganic particulate material. The organic matrix usually determines the chemical properties of the material. Therefore, the chemical selectivity of the sensor device can be controlled by the proper functionalization of the organic matrix. The inorganic, particulate material renders some physical properties to the composite material, which change upon interaction with the analyte, and which, therefore, can be utilized for signal transduction.
M. C. Lonergan et al., Chem. Mater. 1996, 8, 2298-2312, describe chemically sensitive carbon black polymer resistors. Carbon black-organic polymer composites swell reversibly upon exposure to vapors. To obtain a sensor, thin films of carbon black-organic polymer composites were deposited across two metallic leads. Swelling of the film by absorption of vapors induced a change in resistance of the films and signaled the presence of an analyte. To identify and classify vapors, arrays of such vapor-sensing elements were constructed, with each element containing the same carbon black conducting phase but a different organic polymer as the insulating phase. The different gas-solid partition coefficients for the various polymers of the sensor array produced a pattern of resistance changes that can be used to classify vapors and vapor mixtures. This type of sensor array can resolve common organic solvents, including molecules of different classes such as aromatics from alcohols, as well as those within a particular class such as benzene from toluene and methanol from ethanol (see also B. J. Doleman et al., Anal. Chem. 1998, 70, 4177-4190).
G. A. Sotzing et al., Chem. Mater. 2000, 12, 593-595, describe a polyaniline-carbon black chemiresistive detector which can be used to highly sensitive detect and discriminate biogenic amines. Electrically conductive polyaniline is used as the polymeric phase of a carbon black polyaniline composite. Sorption of an odorant into the polymeric phase of the composite produces a characteristic increase in the direct current electrical resistance response of the detector. The response of the detector is approximately six orders of magnitude greater to butylamine than to water, acetone, methanol, ethylacetate, and butanol.
A drawback of the above-described sensors is that, due to the polymeric nature of the sensing material and the rather undefined dispersion of the carbon black particles, it is difficult to control structural features of the material with molecular scale precision. However, the precise control over structural parameters such as inter-particle spacing, position of the analyte-interaction sites relative to the particles, and porosity is highly desirable since this may allow to strongly enhance the sensor's properties as, for example, the chemical sensitivity or the response and recovery times. Moreover, since the carbon black particles may tend to aggregate the composite material may comprise extended regions of high and low conductivity. The size of such regions limits the possibility of device miniaturization. Also the preparation of very thin, homogenous films (<100 nm), which is desirable for enabling short response times may be difficult to achieve.
To overcome such shortcomings ligand-stabilized metal nanoparticles can be used for fabricating chemiresistor films. In this case the ligand shell surrounding the metal cores of the particles provide the organic matrix, which separates the particles from one another. Therefore the inter-particle distance can be precisely controlled through the size of the ligands. Also the molecular structure and the chemical functionality of the ligands can be utilized to tune the electronic transport properties as well as the chemical nature of the composite film. Since the ligand is linked to the nanoparticle surface, the chemical functionality, which serves as the analyte-interaction site, can be precisely positioned with respect to the nanoparticle's surface. Another advantage is that ligand-stabilized nanoparticles can easily be prepared by wet-chemical methods from various metals and with various sizes. This feature can also be exploited to further tune the physical and chemical properties of the films.
S. D. Evans et al., J. Mater. Chem. 2000, 8, 183-188, use para-substituted thiophenol derivatives to stabilize gold nanoparticles. The nature of the substituent group is important for controlling the relative strength of the particle-particle and particle-solvent interactions and hence in determining the physical and chemical properties of these systems. Thin films of the particles were formed by solvent evaporation on microelectrode-patterned surfaces.
The films display ohmic behavior and the room temperature conductivities vary between 10−6 and 10−2 Ω−1 cm−1. Upon exposure to various chemical compounds, the thin films display a change in conductivity. The response to vapors of polar solvents display good repeatability, whereas the response to non-polar organic analytes tends to be less reproducible and displays a variety of time-dependent behavior. Depending upon the nature of the ω-functional group different conductometric and elipsometric responses to the analytes in the vapor phase are displayed. The Au-nanoparticles are not interlinked through linker molecules.
H. Wohltjen and A. W. Snow, Anal. Chem. 1998, 70, 2856-2859, describe a colloidal metal-insulator-metal ensemble chemiresistor sensor based on a monolayer stabilized metal nanocluster transducer film. The thin transducer film is composed of 2 nm gold clusters encapsulated by octanethiol monolayers and is deposited on an interdigitated microelectrode by air-brush technique. Upon exposure to organic vapor, large responses are displayed which are reversible. The sensor is sensitive to non-polar compounds, e.g. toluene and tetrachloroethylene, whereas little response for 1-propanol and water is displayed.
WO 00/00808 describes sensor arrays for detecting an analyte in a fluid. These arrays comprise a plurality of compositionally different sensors. The sensors comprise a conductive material embedded in a matrix of a non-conductive material, e.g. an organic polymer. As a conductive material nanoparticles might be used, that are optionally stabilized by ligand molecules attached to the central core. The ligand molecules can also be polyhomofunctionalized or polyheterofunctionalized. As an insulating material preferably organic polymers are used. It is further suggested to use an alkylthiol ligand as the sole insulating matrix.
Similar sensors and sensor arrays are described in WO 00/33062 and WO 99/08105.
A further sensor is described in FR 2783051. The sensor comprises a nanoparticle film, in which the nanoparticles are stabilized by ligand molecules with at least one functional unit to bind to the nanoparticle surface and at least one functional unit to interact with an analyte molecule.
The sensitive films of such sensors are usually fabricated by applying a solution of ligand-stabilized nanoparticles onto solid substrates and evaporating the solvent. Although the devices show promising features the fabrication of homogenous films with precise control over the film thickness is not easy to achieve by this method rendering the reproducible fabrication and miniaturization of the devices rather difficult. Moreover, the films lack mechanical stability and tend to deteriorate and detach from the substrate, especially when trying to further process the sensor substrate or when applying the sensor to liquids or under harsh environments. The lack of mechanical stability also impairs the overall sensor performance, e.g. baseline and signal stability.
To overcome such shortcomings metal nanoparticle films can be used, which are fabricated by the stepwise layer-by-layer technique described in WO 96/07487. This method is known to produce homogenous multilayered films with nanometer scale control over the average film thickness. Since this method is based on alternated and repeated self-assembly of bi- or polyfunctional linker molecules and nanoparticles the resulting film structures comprise a cross-linked nanoparticle network with greatly improved mechanical stability.
The assembly of a sensor based on self-organisation of nanoparticle-films is described in more detail in WO 99/27357. First a substrate is functionalized with 3-mercaptopropyldimethoxymethylsilane to provide binding sites for the nanoparticles. The activated substrate is then immersed in a solution that contains Au-nanoparticles, which are stabilized by a monolayer shell of alkylthiols. The thiol-groups on the surface of the substrate substitute some of the alkylthiol-ligands bound to the surface of the Au-nanoparticles, thereby attaching the nanoparticles to the surface of the substrate. By subsequently attaching alternating layers of Au-nanoparticles and linker-molecules a thin film is assembled. In the experimental part the use of 1,8-octanedithiol as a linker molecule is described. To modify the sensitivity of the sensor it is suggested to introduce heterofunctionality to the ligand shell. The ligand molecules would then be bifunctional, one functional group to bind with the metal core surface and the other to provide an attractive interaction site for sorption of the target species. It is shown, that the chemical selectivity of the sensor can be influenced by the use of differently functionalized nanoparticles. It is further shown, that the size of the nanoparticles and the thickness of the ligand shell is influencing the chemical sensitivity. The sensors, which were prepared by self-assembly, are found to be most sensitive to toluene, but less sensitive to polar analytes, e.g. propanol and water. When such sensors were exposed to relatively high concentrations of toluene vapor (ca. 2200 ppm) an increase of the resistance of up to 8.2% was reported. We investigated similar chemiresistors made from Au-nanoparticles and nonanedithiol. We observed that such sensors usually responded with a rather weak change of resistance when exposed to various vapors. For example, the relative change of resistance is below 3% when dosing such sensors with 5000 ppm toluene vapor. When applying only 5 ppm toluene vapor, the signal is usually below 0,03% and often difficult to recognize.
Besides the above described chemical sensors based on nanoparticles embedded in an organic matrix organic dentritic compounds have been used to prepare sensitive coatings for mass-sensitive chemical sensor because of their capability to take up guest molecules.
M. Wells and R. M. Crooks, J. Am. Chem. Soc. 1996, 118, 3988-3989 describe the immobilization of poly(amidoamine) (PAMAM) dendrimers onto a surface acoustic wave (SAW) mass balance. Voids within the dendrimer superstructure serve as endoreceptors, and the terminal functional groups of dendrimers serve as exoreceptors. When exposing the SAW-mass balances to volatile organic compounds having different functional groups, a rapid response to the dosants is obtained, wherein the response to the analytes decreases in the order acid>alcohols>hydrophobic dosants. H. Tokuhisa and R. M. Crooks, Langmuir 1997, 13, 5608-5612, could demonstrate, that functionalization of the outer shell of the dendrimers with different organic residues can be used to influence the chemical selectivity of the devices.
WO 97/39041 describes the fabrication of dendrimer monolayers and their application to chemical sensing. In EP 0928813 the preparation and characterization of nanostructured metal/dendrimer composite materials is described.
K. Sooklal et al., Adv. Mater. 1998, 10, 1083-1087 describe the preparation of CdS/dendrimer nanocomposites by the arrested precipitation of nanometer-scale CdS clusters in the presence of PAMAM-dendrimers. The optical properties of the CdS-Clusters are sensitive to synthesis conditions, including dendrimer type, solvent type, and the concentration of dendrimer and other solutes. Thin films of these CdS/dendrimer nanocomposites were prepared by casting solutions onto frosted microscope slides followed by solvent evaporation. Those thin films retain approximately the optical properties of their parent solutions. V. Chechik et al., Langmuir 1999, 15, 6364-6369, describe the synthesis of fourth-generation PAMAM-dendrimers having terminal groups partially or fully functionalized with thiol groups. These thiolated dendrimers form stable monolayers on planar Au-substrates. In monolayers of partially functionalized dendrimers most of the thiol groups directly interact with the Au surface. Thiol-modified dendrimers also act as efficient stabilizers for Au-nanoparticles. The particles obtained are small (1-2 nm) even when the reduction is carried out in the presence of an excess of the Au-salt. Such nanocomposites are stable and can be isolated in a pure form by gel filtration.
M. E. Garcia, L. A. Baker, R. M. Crooks, Anal. Chem. 1999, 71, 256-258, describe the preparation and characterization of dendrimer-gold colloid nanocomposites. Au colloids in the 2-3 nm size regime can be prepared by in situ reduction of HAuCl4 in the presence of poly(amidoamine) (PAMAM) dendrimers. The dendrimers encapsulate the colloids, imparting stability to the aqueous colloidal solutions. The nanocomposite materials can be isolated by precipitation. The size of the resultant colloids is controlled by the dendrimer generation: lower generation dendrimers give rise to larger colloids.
Compared to mass sensitive chemical sensors, signal transduction and signal readout of chemiresistors is simpler and allows for easier device miniaturization and integration, especially when aiming for integration of extended sensor arrays into silicon based circuits.
It therefore is an object of the invention to provide a chemical sensor with selectivity towards target analytes, high sensitivity, simple and robust signal transduction, and high stability in performance.
To solve this object, the present invention provides a chemical sensor, comprising a substrate, a sensor medium formed on the substrate, and detection means for detecting a change of a physical property of the sensor medium, wherein the sensor medium comprises a network formed of non-linear polymer or oligomer molecules having linker units and of particles of at least one second component, wherein the linker units are bound to the surface of the particles of the at least one second component thereby interlinking said particles.
As non-linear polymer or oligomer molecules might be used star-polymers, comb-polymers, hyperbranched polymers and dendrimers. Star polymers are polymers having a more or less spherical shape provided with several arms. To a core are linked linear polymers, which spread radially outward. Comb-polymers have a linear backbone, which is formed as a linear polymer. To the backbone are connected linear polymers which spread sidewards from the molecule backbone and form side-chains. Hyperbranched polymers have a structure similar to the polymers described above but the polymers connected to the core or the backbone of the molecule are branched. The linker units form part of the polymers and are preferably situated at the terminating end of the polymer chain.
Best suited to carry out the invention are dendrimer molecules. In the following the invention will be discussed in more detail with reference to dendrimer molecules. But a chemical sensor according to the invention might also be assembled on the basis of the other non-linear polymers or oligomers mentioned above.
The chemical sensor according to the invention provides a sensor device with high sensitivity and good mechanical stability, achieved by cross-linking the components of the sensor medium with functionalized dendrimers. The use of dendrimers, which provide sites of interaction with analyte molecules, also enables tuning the chemical sensitivity through proper functionalization of the dendrimer structure. The size and structure of the dendrimer component can also be used to control the porosity of the film material. Cross-linking of the sensor medium components enables the precise control of the sensor medium architecture, e.g. the film thickness and interparticle spacings, during sensor fabrication, which improves the reproducibility of device fabrication. To obtain a fast response and a high sensitivity the sensor medium is generally formed on the substrate as a film having a thickness of around ten nanometres to few micrometers.
Dendrimers are quasi-spherical organic polymers or oligomers that have well-defined structures with less dense interiors and densely packed surfaces, especially in the case of higher generation dendrimers. General information on the physical and chemical properties and the structures of dendrimers may be found in G. R. Newkome, C. N. Moorefiled, F. Voegtle, “Dentritic Molecules: Concepts, Synthesis, Perspectives”, VCH, 1996, Weinheim, Germany. The preparation and characterization of nanoparticle/dendrimer composite materials has been described e.g. in R. M. Crooks, B. I. Lemon III, L. Sun, I. K. Yeung, M. Zhao, Top. Curr. Chem. 2001, 212, 81-135; M. Zhao, L. Sun, R. M. Crooks, J. Am. Chem. Soc. 1998, 120, 4877-4878; K. Sooklal, L. H. Hanus, H. J. Ploehn, C. J. Murphy, Adv. Mater. 1998, 10, 1083-1087; G. Bar, S. Rubin, R. W. Cutts, T. N. Taylor, T. A. J. Zawodzinski, Langmuir 1996, 12, 1172-1179; R. M. Crooks, M. Zhao, L. Sun, V. Chechik, I. K. Yeung, Acc. Chem. Res. 2001, 34, 181-190; M. E. Garcia, L. A. Baker, R. M. Crooks, Anal. Chem. 1999, 71, 256-258; V. Chechik, R. M. Crooks, Langmuir 1999, 15, 6364-6369; K. Esumi, A. Suzuki, N. Aihara, K. Usui, K. Torigoe, Langmuir 1998, 14, 3157-3159; and EP 0 928 813.
Depending on the structure of the molecules different types of dendrimers, dendrons or dentritic compounds are known. All these compounds may be used for assembling a chemical sensor according to the invention and are generally called “dendrimers” or “dendrimer molecules” in the following.
The dendrimer component fulfils one of the following functions or properties or any combination thereof:
a) Molecularly designed porosity of the nanoparticle film, which enables the uptake and diffusion of analyte within the composite material. This can be utilized to improve the sensor's sensitivity and response time and to tune the selectivity of the sensor device by providing a size-selective filter effect.
b) Cross-linking other components of the composite (such as nanoparticles, oligomers, polymers) to give mechanical stability;
c) Tuning the chemical nature of the composite material and, thereby, the chemical selectivity of the intended sensor device by utilizing the chemical properties of the dendrimer's interior and/or of its surface;
d) The dendrimer may also provide some physical properties that can be used for signal transduction (e.g. luminescence, absorbance).
With respect to the invention, the dendrimer structure may be roughly divided into four parts: A core (or focal point), which forms the central part, a shell of branched repeating units, another shell of spacer units, and an outer shell of linker units, which serve to cross-link other components of the composite material.
Dendrimer structures, which are either flexible or rigid and open favor the uptake of analyte molecules by the composite material and therefore can enhance the sensitivity of the sensor device. Flexible structures usually comprise a relatively high content of sp3-hybridized carbon (and/or hetero) atoms and have a high degree of conformational freedom. In contrast, rigid structures usually comprise a high content of unsaturated sp- and/or sp2-hybridized carbon (and/or hetero) atoms, preferably at least 40% of the carbon atoms of the core and the shell of branched repeating units are sp2 and/or sp hybridized, and the degree of conformational freedom is limited (e.g. by sterical hindrance). However, rigid dendrimer structures may also be made from sp3-carbon rich cage-like compounds (e.g. adamantane and ist derivatives, cyclodextrines, metal ion/crown ether complexes, metal ion/polyether complexes), or may comprise porphyrin or phthalocyanin (which may be complexed with a metal ion), or derivatives thereof. The uptake of analyte species by flexible dendrimers is accompanied by a change of the dendrimer's shape and volume, whereas rigid dendrimers do not swell when interacting with the analytes. The chemical nature of the dendrimer interior strongly determines the chemical selectivity of the composite material. Functional groups of the interior structure, which can interact with the analyte molecules act as endo-receptor sites. In general, polar functional groups of the dendrimer's interior tune the chemical selectivity towards polar analyte molecules, whereas non-polar functional groups (or non-polar residues) favor selectivity for non-polar analytes. Tab. 1 shows structural units that are preferably used to form the core structure and the repeating units of the dendrimer. The structural units listed in the table may be used in any combination to form the core structure and the repeating units of the dendrimer.
Structural units used to form the core structure
and the repeating units of dendrimers
The groups displayed in the first two lines of table 1 comprise at least three valences (*) and therefore may act as branching units and as endo-receptor sites, whereas those groups having two valences (*)act as endo-receptor sites, e.g. an imino- or an azogroup, enabling selective interaction with certain analytes. A phenyl ring may carry up to 6 branches and also may carry substituents, e.g. halogen atoms, hydroxy groups, or an organic residue, such as alkyl or alkoxy groups. X represents such substituents.
The structure of the dendrimer core and the repeating units may comprise electron-donating groups, e.g. amino groups, imino groups, aromatic groups comprising hetero atoms (N, S, O), carbonyl groups, carboxy groups, ether groups, thio groups, etc., which may be used for complexing metal cations. Suitable metal cations may be main group metals, such as Mg2+, Ca2+, Pb2+, etc., transition metals, such as Mn2+Co2+, Ru2+, Fe2+, Fe3+, Cu2+, Ag+, Zn2+, Cd2+, Hg2+, Cr3+, Pt2+, Au3+, Pd2+, etc., rare earth metals, such as Ce3+, Eu3+, etc., which themselves can serve to form selective interaction sites for analytes, e.g. O2, CO, NH3, SOx, NOx. Examples of metallodendrimers are given in G. R. Newkome, E. He, C. N. Moorefield, Chem. Rev. 1999, 99, 1689-1746. Amine units may also be protonated to form a cationic interaction site.
In order to enhance the selective interaction with certain analytes the repeating units may also be functionalized with terminating structural units. The valences of the structural units, which are not involved in linking these units to the dendrimer structure may carry a hydrogen atom or a small alkyl group, e.g. a methyl or an ethyl group, a small alkoxy group, e.g. methoxy, ethoxy, or may be deprotonated to form an ionic unit. Such terminating units may also be formed from the units given in Table 3 below.
The functional and structural units of the dendrimer may be arranged in such a way, that more than one unit can interact with the same analyte. Such a concerted interaction can strongly enhance the selectivity. Moreover the interaction sites may be arranged sterically in such a way, that they enable stereo-selective sensing, e.g. of chiral compounds.
Chemically bonded to the shell of repeating units may be a shell of spacer units. These units are structural units, which mainly serve to functionalize the outer sphere of the dendrimer with terminal linker units. Examples for structural units that may be used to form the spacer units of the dendrimers are given below in table 2. These units may be used in any combination to form the spacer units.
Structural units used to form the spacer units of
The structure of the spacer is preferably formed by alkylene, alkenylene or alkinylene groups at least comprising 3 carbon atoms. For binding the spacer to the shell of repeating units, both parts comprise suitable functional or structural groups. For example such units may form an ester linkage or an amide linkage.
The spacers carry functional groups and/or structural units at their ends that act as linker units to cross-link the dendrimers to other (second) components of the composite. Preferably the linker units are formed by polar groups and/or sulphur-containing groups. Table 3 shows preferred examples of structural units that may be used to form linker units of the dendrite molecules.
Structural units used to form the linker units of
Some of the valences of the groups shown in table 3 may be terminated by a hydrogen atom thereby forming e.g. a terminating hydroxyl group, amine group or thiol group, or may be deprotonated and form for example a thiolate or carboxylate group.
The dendrimer preferably cross-links other components of the composite material through covalent bonds or coordinative bonds (e.g. metal-ligand such as Au/thiol). But linking of the dendrimer molecules may also be obtained through non-covalent bonding, such as ionic or dipole-dipole interactions or metal-ion complexation. In case the dendrimer molecules are attached to the surface of a metal particle or a semiconductor particle it is preferred, that the dendrimer molecules comprise an outer shell of suitable linker units forming the surface of the dendrimer molecule. The linker units may be coupled to the dendrimer molecule by appropriate spacer units. Preferably the linker units are selected from the group formed of thiol groups, disulfide groups, amino groups, isocyanide groups, thiocarbamate groups, dithiocarbamate groups, chelating polyether, and carboxy groups. Within the dendrimer molecule the linker units may be of the same or of different type. Polar linker units, that are not bound to the second component may also act as exo-receptors for analytes.
The structure of the dendrimer (especially the repeating units, the spacer units, and/or the linker units) may comprise or may be formed from amino acids, e.g. glycine (GLY), alanine (Ala), valine (Val), leucine (Leu), isoleucine (Ile), methionine (Met), proline (Pro), phenylalanine (Phe), tryptophan (Trp), serine (Ser), threonine (Thr), cysteine (Cys), tyrosine (Tyr), asparagine (Asn), glutamine (Gln), aspartic acid (Asp), glutamic acid (Glu), lysine (Lys), arginine (Art), histidine (His), or nucleotides, or nucleotide -building blocks, e.g. cytosine, uracil, thymine, adenine, guanine, ribose, 2-deoxyribose, or derivatives of such compounds.
If the sensing material is used for detecting non-polar analytes, the chemical nature of the dendrimer, especially the dendrimer interior structure, should also be non-polar. Preferred non-polar dendrimer structures comprise phenyl- or polyphenylene units, which are connected with each other through carbon bonds and/or ether bonds. Such dendrimers can be rather rigid and comprise defined voids in their interior, which can take up guest molecules.
If the sensing material is used for detecting polar analytes, the chemical nature of the dendrimer, especially the dendrimer interior structure, should also be polar. Because of their commercial availability a preferred dendrimer used for assembling of the sensor film is a polyamidoamine (PAMAM) dendrimer. Further preferred dendrimers that can be obtained from commercial sources are poly(propylene imine) (PPI) dendrimers. Those dendrimer molecules are available in different sizes depending on the generation of the dendrimer (e.g. generation-1 to generation-8). Those dendrimers of different generation differ in their physical and chemical properties and may therefore be used to modify the selectivity and/or sensitivity of the chemical sensor.
In both PAMAM and PPI dendrimer structures the branching positions are formed of nitrogen atoms. Also, both structures are pretty flexible, since the structural units comprise a high content of sp3-hybridized atoms with a high degree of rotational freedom. Since in both cases the structure contains polar functional groups (amide- or amine-groups) these dendrimers are suited for the fabrication of sensors with selectivity for polar, hydrophilic analytes, especially the PAMAM-dendrimers, which contain hydrophilic amide groups, that can act as endo-receptors. Sensors based on PPI-dendrimers are especially selective to acidic analytes, because of the amine functional groups.
Both PAMAM- and PPI-dendrimers can incorporate (complex) metal cations (e.g. Ag+, Au3+, Pt2+, Pd2+, Cu2+). Furthermore the metal cations can be reduced by UV-irradiation or by wet-chemical methods to form dendrimer stabilized metal nanoparticles. Also semiconductor materials can form clusters with such dendrimer molecules, e.g. PAMAM-stabilized CdS clusters. Nanoparticles might therefore be used as second component of the sensor medium. Stabilization of the nanoparticles by dendrimers is achieved by adsorption of the dendrimers on the nanoparticle's surface. The amino groups on the dendrimer's outer sphere serve as linker units to bind to the surface of the nanoparticles. Since the amino groups have a high affinity for many metal surfaces PAMAM-dendrimers form monolayers on metal substrates (e.g. Au substrates). Further the primary amino groups of PPI and PAMAM-dendrimers can be used to covalently attach the dendrimer to self-assembled monolayers of organic thiols, as described by Wells and Crooks (M. Wells, R. M. Crooks, J. Am. Chem. Soc. 1996, 118, 3988-3989).
The chemical nature of the outer sphere of PPI- and PAMAM-dendrimers can be controlled by coupling various organic residues as exo-receptors to the primary amino groups via amide coupling. This can be utilized to tune the chemical selectivity of dendrimer based sensors and/or to improve the coupling of the dendrimer molecules e.g. to the surface of a nanoparticle. This might be achieved by providing e.g. a thiol group or a disulfide group on the surface of the dendrimer molecule by coupling such linker units to the terminal amino groups through an appropriate spacer unit by an amide bond. An example, which demonstrates how PAMAM-dendrimers can be functionalized with terminal thiol groups has been described by V. Chechik et al., Langmuir 1999, 15, 6364-6369. Other terminal groups, which are useful to bind to many metal nanoparticles, were already given above in Table 3. PAMAM-dendrimers are also available with hydroxy termination (instead of amino termination). These dendrimers are referred to as PAMAM-OH (Sigma-Aldrich). Also carboxy-terminated PAMAM-dendrimers are commercially available. All these PAMAM-dendrimers can be used to prepare highly cross-linked dendrimer/polymer composite materials, which are useful as sensor media. The dendrimer's amino-, hydroxyl-, or carboxy-groups are utilized to cross-link the polymer components of the composite material.
Preferred is the use of dendrimer composite materials as a chemical sensor, which utilizes a change of the optical or, especially preferred, the electronic properties for signal transduction. To provide such useful optical and/or electronic properties to the composite material, nanoparticles can be used as a second component.
Nanoparticles are nanoscopic objects that are confined in at least one dimension to the nanometer scale (<1000 nm, preferably <100 nm). Thus, nanoparticles may resemble spheres (3-dimensional confinement), fibers or tubes (2-dimensional confinement) or sheets (1-dimensional confinement). Examples for 3-dimensionally confined nanoparticles are surfactant-stabilized metal and semiconductor nanoparticles, and fullerenes, such as C60. Examples for 2-dimensionally confined nanoparticles are carbon nanotubes, and semiconductor nanofibers, such as V2O5-nanofibers. Examples for 1-dimensionally confined nanoparticles are sheets made from ZnS or titania. All those nanoparticles may be used in the assembly of the chemical sensor. Preferred is the use of three-dimensionally confined nanoparticles in the size regime between 0.8 to 100 nm.
In general nanoparticles may consist of insulating material, however for providing useful optical and/or electronical properties they preferably consist of semiconducting material, or metal. Such nanoparticles can be prepared by various methods, ranging from gas-phase techniques to wet-chemical synthesis, which have been described by numerous papers in the literature. The wet-chemical preparation methods usually provide ligand-stabilized and/or charge-stabilized nanoparticle solutions. Such preparation methods are well known to persons skilled in the art.
The nanoparticles fulfil two different tasks. First, they strongly determine the physical properties of the composite film material, which are measured when operating the sensor. If the sensing principle requires electric conductivity, then metal particles are preferred because they strongly enhance the electric conductivity of the material. This allows, for example, measuring changes of the electric conductivity as the sensor signal. As a rule of thumb, the use of larger particles leads to films with higher conductivity than using smaller ones. Moreover, many metal and semiconductor nanoparticles have pronounced optical properties (absorption and/or luminescence), which may change upon interaction of the analyte with the film material. Second, the nanoparticles serve as nanoscopic substrates for binding the dendrimer molecules. In this sense, the nanoparticles can be considered as junctions of the nanoparticle/dendrimer network. These nanoparticle networks comprise cavities in-between the nanoparticles, which support the diffusion of analyte species into the sensor film material.
It is mentioned that when using the sensor device for detecting certain target analytes, the nanoparticle material may also be used to tune the chemical selectivity of the film. For example, many metal nanoparticles can strongly interact with gases as CO, NH3, NOx, SOx, etc. These interactions can induce strong changes of the optical and/or electronic properties, which can be used as the sensor's signal.
For the use of the nanoparticle film as a chemiresistor, an important function of the nanoparticles is to provide sufficient conductivity. Therefore, the nanoparticle preferably is a metal nanoparticle. Metals suited for the fabrication of a nanoparticle sensor film are preferably selected from the group consisting of Au, Ag, Pt, Pd, Cu, Co, Ni, Cr, Mo, Zr, Nb, and Fe. It is also possible to use nanoparticles comprising combinations (e.g. alloys) of these metals.
It is also possible to use semiconductor nanoparticles (e.g. II/VI semiconductors such as CdS, CdSe, CdTe, ZnO, ZnS, ZnSe, ZnTe, HgS, HgSe, HgTe, or III/V semiconductors such as GaAs, InAsInP, or others such as PbS, Cd3P2, TiO2, V2O5, SnO and other transition metal oxides, or combinations of these materials, including core/shell structures, e.g. CdS/CdSe or CdSe/ZnS. In order to enhance the conductivity of the semiconductor nanoparticles, they may be doped (e.g. As, Sb, Al, B, P, In, Lanthanides, transition metals). In this case the dendrimers serve to interlink the nanoparticles. Semiconductor nanoparticles provide properties that can be used for optical and/or electrical signal transduction and, therefore, for the fabrication of chemical sensors.
Further, also combinations of metals, semiconductors, and/or insulators may be used as nanoparticles. As insulator materials might be used SiO2, Al2O3 or MgO. Nanoparticles solely consisting of insulator materials might also be used for assembling the sensor media according to the invention.
In principle, it is also possible to provide conducting or semiconducting particles from conducting organic materials such as conducting polymers. It is understood that the nanoparticles mentioned here can also be used in any combination for preparing the sensitive materials.
In order to provide useful electronic properties to the dendrimer composite material it is also possible to combine the dendrimer component with (semi)conducting polymers or oligomers instead of (or in addition to) the above described nanoparticles. The fabrication of dendrimer/polymer composites has already been described by M. Zhao, Y. Liu, R. M. Crooks, D. E. Bergbreiter, J. Am. Chem. Soc. 1999, 121, 923-930, and WO/9858970. (Semi)conducting polymers or oligomers, which are useful to provide useful electronic properties to the dendrimer composite material are for example polypyrrole, polyaniline, polythiophene, or any derivatives of these polymers. Other examples of semiconducting polymers are described in G. Hadziioannou, P. F. van Hutten (Eds.): “Semiconducting Polymers—Chemistry, Physics and Engineering”, Wiley-VCH, Weinheim, Germany. Such sensor media can be fabricated by reacting the terminal functional groups of a dendrimer with functional groups of a (semi)conducting polymer (or semiconducting oligomer). Dendrimers that are suitable for this purpose may have a polar or non-polar molecular structure, tuning the chemical selectivity towards polar or non-polar analytes, respectively. The dendrimers serve to cross-link the semiconducting polymer component.
The chemical sensor according to the invention may be used in various types of chemical sensor devices that use different physical properties to detect an analyte. In a first group, a change of an electrical property is detected. For example, a change in conductivity or capacity of the sensor film may be measured. Therefore, the chemical sensor may act as a chemiresistor or a chemicapacitor. The sensor film can also be utilized in a configuration forming a chemidiode or a multiterminal device, such as a chemitransistor (e.g. Chem-FET). Examples of chemical sensitive transistors comprising semiconducting oligomers based on polythiophene have recently been described in the literature (B. Crone, A. Dodabalapur, A. Gelperin, L. Torsi, H. E. Katz, A. J. Lovinger, Z. Bao, Appl. Phys. Lett. 2001, 78, 2229-2231). The chemical sensor may also be used as a mass sensitive sensor. The nanoparticle film is then used as a coating on a piezo-electric material to form a chemically sensitive surface acoustic wave (SAW) device or a quartz crystal microbalance (QCM).
According to another embodiment, the chemical sensor is used as an optical sensor. The sensor signal may then be measured as a change in reflectance, fluorescence, absorption, or scattering. In this case, the binding of analyte molecules to the sensor material leads to a change of optical properties (UV/vis and/or IR). Suitable materials may comprise, for example, semiconductor nanoparticles, which show electro- and or photo-luminescence. For example, the luminescence properties may change when the analyte molecules are adsorbed to the dendrimer/nanoparticle material. This change is due to a change of the electronic states of the nanoparticles and/or of the close environment of the nanoparticles (i.e. the electronic states of the dendrimers or of the analyte itself). Examples of suitable semiconductor materials were already given above.
It is also possible to utilize the sensor films as chemically sensitive coatings for fiber optics (e.g. optodes, interferometer devices). The chemical sensor may also use changes in heat or temperature and therefore be used as a thermistor, or other thermoelectric device.
Preferably the chemical sensor is formed as a chemiresistor, wherein the sensor medium is deposited as a film on a pair of contacting electrodes.
The sensor film may be deposited onto electrodes, e.g. made of Au, which were deposited on an inert substrate, e.g. by lithographic techniques, or both electrodes may be deposited on top of the film. Also other configurations are possible. One electrode may be positioned below the sensor film and the other may be deposited on top of the sensor film. By the sorption of the analyte to the dendrimer composite material the electronic properties of the sensor are influenced resulting in a change of conductivity of the sensor film.
The inert substrate can be made for example of Si/SiO2 when the chemical sensor is integrated in an IC device. Further preferred substrates are made of glass and/or ceramics.
Several chemical sensors, which preferably have different compositions of the sensor film, may be arranged to form a sensor array.
The chemical sensor according to the invention may be miniaturized, e.g. to be used in a sensor array in an IC device.
The chemical sensor comprises at least one nanoparticle and at least one dendrimer molecule.
The chemical sensor may comprise a single nanoparticle to which two dendrimer molecules are attached. The dendrimer molecules may then be attached e.g. to electrodes with a further linker unit.
According to another embodiment, the chemical sensor may comprise a single dendrimer molecule, which is attached to two nanoparticles.
The sensor film containing nanoparticles may be formed by a one-step procedure as described by F. L. Leibowitz, W. Zheng, M. M. Maye, C.-J. Zhong, Anal. Chem. 1999, 71, 5076-5083, who investigated the formation and properties of Au-nanoparticle/alkyldithiol films. This method is based on precipitating the film material by mixing the nanoparticles and the linker molecules in solution phase in the presence of the substrate. Thus, mixing dendrimers having suitable linker units at their surface with suitable nanoparticles results in the precipitation of a thin film composite material. However, to obtain stable nanoparticle films with high precision, the nanoparticle film is preferably prepared through layer-by-layer deposition of the nanoparticles. This procedure has been described in principle by D. Bethell, M. Brust, D. J. Schiffrin, C. Kiely, J. Electroanal. Chem. 1996, 409, 137-143; M. Brust, D. Bethell, C. J. Kiely, D. J. Schiffrin, Langmuir 1998, 14, 5424-5429, and in WO 96/07487. In the case of the present invention, the assembly of the nanoparticle film occurs through stepwise self-organization organization of the nanoparticles and of the dendrimer molecules. This allows the formation of nanoparticle sensor films under more controlled and reproducible conditions.
A further subject of the invention therefore is a method for forming a chemical sensor as described above, comprising the following steps:
Preferably dendrimer molecules are used as non-linear polymers.
Preferably the substrate is first functionalized to provide linker groups on the surface of the substrate. In a preferred embodiment the method for forming a chemical sensor comprises the following steps:
a) functionalization of a substrate to provide linker groups on the surface of the substrate;
b) deposition of a layer of nanoparticles on the functionalized substrate surface theeby linking the nanoparticles to the linker groups;
c) deposition of dendrimer molecules on the layer of nanoparticles and coupling of the dendrimer molecules to the nanoparticles;
d) deposition of a further layer of nanoparticles and linking them through the dendrimer molecules with the nanoparticles of the first layer;
e) repeating steps c) and d) until a homogenous sensor film of nanoparticles is obtained.
The deposition of the nanoparticles and the deposition of the dendrimer molecules is repeated until a nanoparticle sensor film is obtained which has sufficient conductivity for being used as a chemiresistor (preferably R<10 MΩ). The deposition of the nanoparticles and of the dendrimer molecules may be performed by any suitable method. The nanoparticles or the dendrimer molecules may be deposited by spraying or dipping with a solution of the nanoparticles or of the dendrimer molecules in a suitable solvent and evaporation of the solvent or by a spin-coating technique. Usually the nanoparticles are applied in the form of a solution of ligand-stabilized nanoparticles. Binding of ligand or dendrimer molecules is achieved via ligand-exchange reactions. In such exchange reactions, at least some of the stabilizing ligands are exchanged by the dendrimer molecules. For example, dodecylamine ligands on the surface of Au-nanoparticles are easily exchanged by thiol functionalized dendrimer molecules. The functionalization of the substrate might be performed by e.g. coupling a mercapto- or aminoalkylsilane to the surface of the substrate.
As the last step in the formation of the sensor film preferably a layer of dendrimer molecules is depositet, so that the surface of the sensor film is formed by dendrimer molecules.
According to another embodiment of the method according to the invention the chemical sensor is produced by a method, wherein a mixture comprising non-linear polymers having linker units, nanoparticles and a solvent is prepared on the surface of a substrate or is applied to the surface of a substrate, and the solvent is removed to form a film of a sensor medium.
Also in this embodiment the surface of the substrate may first be functionalized to provide linker units on the surface of the substrate.
The above-described sensor may be used for the detection of analyte molecules in gas or solution phase. A further subject of the invention therefore is a method for detecting an analyte, wherein the sensor medium of a chemical sensor as described above is exposed to the analyte and a change of a physical property of the sensor film is measured by a detection means. The change of a physical property may be e.g. a change in conductivity, dielectric constant, reflectance, color, luminescence, absorbance, mass, volume, density, and/or heat capacity.
The invention will now be described in more detail by way of examples and with reference to the accompanying figures.
The general structure of dendrimers, which can be used to assemble a chemical sensor according to the invention, is schematically shown in
According to the number of arms of the core 1, the dendrimer structure may be divided into segments 5 as shown in
A dendrimer molecule corresponding to the general description above is depicted in
Besides the thioctic acid residues R also other spacer and/or linker units may be used. Examples of such groups are also depicted in
Another example of a dendrimer that can be used for assembling chemical sensors according to the invention is shown in
Also the dendrimer shown in
In both dendrimer structures, which are shown in
A constant current may be applied to the leads 9 of the electrodes and a change in the voltage across the electrodes may be detected by a detector (not shown). The detailed part of the figure shows the nanoparticles 10 interlinked through dendrimer molecules 11 thereby forming a dendrimer/nanoparticle network.
A wet-chemical method previously described by Leff et al., Langmuir 1996, 12, 4723-4730, was used to prepare a colloidal solution of dodecylamine-stabilized Au-nanoparticles. To a rapidly stirred solution of 160 mg AuCl3 in 20 ml water a solution of 639 mg tetraoctylammoniumbromide in 20 ml toluene was added. It was stirred until the organic phase turned into red-orange, while the aqueous phase turned colourless. To the mixture 1178 mg dodecylamine and 30 ml toluene were added. Under vigorous stirring a freshly prepared solution of 221 mg NaBH4 in 15 ml water was added. The colour of the solution immediately turned into deep purple. After stirring over night under ambient conditions the organic phase was separated and 40 ml ethanol were added. The mixture was stored in the freezer at −18° C. over night. By filtration through a nylon membrane (0,45 μm pore size) the precipitate was separated from the solution and redissolved in about 20 ml toluene. This solution was subjected to fractionated precipitation, which was done by repeating the following three steps: 1. Addition of ethanol (ca. 40 ml), 2. Letting sit over night in a freezer, 3. Separation of the precipitate by centrifugation or filtration. This way four fractions were obtained, from which fraction 2 was used for sensor fabrication. TEM analysis of fraction 2 revealed that the Au-nanoparticles were crystalline and had an average diameter of 3.9 nm with a standard deviation of 1.2 nm. A TEM micrograph is shown in
Fabrication and characterization of an electrically addressable polyphenylene-dendrimer/Au-nanoparticle composite film:
For assembling a sensor film a dendrimer having a structure as depicted in
Fabrication of electrically addressable PAMAM-dendrimer/Au-nanoparticle and PPI-dendrimer/Au-nanoparticle films:
Similar as described above, we prepared PAMAM- and PPI-dendrimer/Au-nanoparticle composite films. As the only differences we used solutions of 10 mg PAMAM-G4 (generation-4) or PPI-G3 (generation-3) dendrimers in 5 ml methanol instead of the polyphenylene dendrimer solution.
After each exposure of the substrates to the dendrimer solutions, the substrates were first rinsed with methanol and then with toluene, before exposing them to the Au-nanoparticle solutions. Accordingly, after exposing the substrates to the nanoparticle solutions, they were first rinsed with toluene and then with methanol before exposure to the dendrimer solutions. It is noted that the PAMAM- and PPI-dendrimers we used comprised 64 and 16 primary surface amino groups, respectively, which served as linker units to cross-link the Au-nanoparticles.
Vapor sensing properties of the polyphenylene-dendrimer/Au-nanoparticle film:
Comparison of the vapor-sensing properties of a polyphenylene-dendrimer/Au-nanoparticle film resitor, a PAMAM-dendrimer/Au-nanoparticle film resistor, and a PPI-dendrimer/Au-nanoparticle film resistor:
Equipment used for sensor characterization:
The vapor-sensing properties of the Au-nanoparticle/dendrimer composite films were investigated by exposing the film to various solvent vapors while measuring the change of resistance as the sensors' signal. For dosing the sensors with the test vapors, we used a gold plated aluminum chamber, equipped with pogo pin contacts pressing onto the contact pads of the electrode structures. The chamber was equipped with a meandering heat-exchange channel for thermally equilibrating the test vapors. Since we observed that operating the sensors at elevated temperatures improved the sensors' recovery after vapor exposure, we kept the temperature of the test chamber constant at 39° C. in all experiments. Moreover, in order to remove contaminants from the sensor's surfaces the devices were kept in vacuum (ca 8 mbar) for about six hours before each experimental run. Usually the sensors were operated by applying a constant direct current (using a Keithley Source-Measure-Unit 236) and measuring the change of voltage across the electrodes (using a Keithley 2002 Multimeter) while applying a test gas atmosphere. The sensors were operated at a bias below 1V. Vapors of solvents were generated with commercial gas calibration systems (Kalibriersystem MK15/MK5 or MK15-DDS-RL/MK5, Umwelttechnik MCZ GmbH, Ober-Mörlen, Germany). These systems comprise bubblers and condensers for preparing saturated solvent vapors in a temperature range between 15 to 50° C. By using several mass flow controllers the saturated vapors were diluted with zero-gas to a concentration range of 1 to 5000 ppm (ppm=volume parts per million). As zero gas we used purified and dried air (dew point −70° C.), which was provided by a commercial zero-gas generator (Nullgasanlage MD2000-25, Umwelttechnik MCZ), equipped with a catalytic purification unit. The mass flow system was equipped with a computer-controlled valve for switching the gas flow through the sensor cell between zero-gas and test gas. As test-gas vapors we used toluene, tetrachloroethylene (TCE), 1-propanol, and water. The actual concentrations of the vapors in the test cell were calculated by using the Antoine equation and the dilution factors adjusted by the mass flow system. The mass flow in the test chamber was adjusted to 400 mL/min and kept constant for all experiments.
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|U.S. Classification||436/169, 422/82.02, 422/68.1, 422/82.01, 422/82.05|
|International Classification||G01N21/77, G01N21/27, G01N33/543, G01N27/22, C09K3/00, G01N5/02, G01N33/00, G01N21/64, G01N27/12, G01N30/00|
|Cooperative Classification||B82Y15/00, G01N21/77, Y10T436/11, G01N33/0001, G01N27/126|
|European Classification||G01N27/12E2, G01N33/00B, G01N21/77|
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